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Peter M Andersen

Showing results (201-210 of 241) with videos related to

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Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Neurobiology of Aging|October 16, 2012
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosisWouter van Rheenen, Frank P Diekstra, Perry T C van Doormaal, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 15, 2016
Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALSPatrick Oeckl, Claude Jardel, François Salachas, et al.
Human Molecular Genetics|November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosisAn Goris, Jessica van Setten, Frank Diekstra, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 10, 2023
Clinical testing panels for ALS: global distribution, consistency, and challengesAllison A Dilliott, Ahmad Al Nasser, Marwa Elnagheeb, et al.
Brain : a Journal of Neurology|October 16, 2019
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutationsDavid Brenner, Angela Rosenbohm, Rüstem Yilmaz, et al.
European Journal of Epidemiology|March 13, 2016
Physical activity and risk of Amyotrophic Lateral Sclerosis in a prospective cohort studyValentina Gallo, Nicola Vanacore, H Bas Bueno-de-Mesquita, et al.
Annals of Neurology|January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease SeverityMatthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2025
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implicationsAlfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Pageof 25

Showing results (201-210 of 241) with videos related to

Sort By:
Pageof 25
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Neurobiology of Aging|October 16, 2012
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosisWouter van Rheenen, Frank P Diekstra, Perry T C van Doormaal, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 15, 2016
Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALSPatrick Oeckl, Claude Jardel, François Salachas, et al.
Human Molecular Genetics|November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosisAn Goris, Jessica van Setten, Frank Diekstra, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 10, 2023
Clinical testing panels for ALS: global distribution, consistency, and challengesAllison A Dilliott, Ahmad Al Nasser, Marwa Elnagheeb, et al.
Brain : a Journal of Neurology|October 16, 2019
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutationsDavid Brenner, Angela Rosenbohm, Rüstem Yilmaz, et al.
European Journal of Epidemiology|March 13, 2016
Physical activity and risk of Amyotrophic Lateral Sclerosis in a prospective cohort studyValentina Gallo, Nicola Vanacore, H Bas Bueno-de-Mesquita, et al.
Annals of Neurology|January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease SeverityMatthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2025
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implicationsAlfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Pageof 25